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Small Nerve Fiber Pathology in Critical Illness

BACKGROUND: Degeneration of intraepidermal nerve fibers (IENF) is a hallmark of small fiber neuropathy of different etiology, whose clinical picture is dominated by neuropathic pain. It is unknown if critical illness can affect IENF. METHODS: We enrolled 14 adult neurocritical care patients with pro...

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Autores principales: Latronico, Nicola, Filosto, Massimiliano, Fagoni, Nazzareno, Gheza, Laura, Guarneri, Bruno, Todeschini, Alice, Lombardi, Raffaella, Padovani, Alessandro, Lauria, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3787101/
https://www.ncbi.nlm.nih.gov/pubmed/24098716
http://dx.doi.org/10.1371/journal.pone.0075696
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author Latronico, Nicola
Filosto, Massimiliano
Fagoni, Nazzareno
Gheza, Laura
Guarneri, Bruno
Todeschini, Alice
Lombardi, Raffaella
Padovani, Alessandro
Lauria, Giuseppe
author_facet Latronico, Nicola
Filosto, Massimiliano
Fagoni, Nazzareno
Gheza, Laura
Guarneri, Bruno
Todeschini, Alice
Lombardi, Raffaella
Padovani, Alessandro
Lauria, Giuseppe
author_sort Latronico, Nicola
collection PubMed
description BACKGROUND: Degeneration of intraepidermal nerve fibers (IENF) is a hallmark of small fiber neuropathy of different etiology, whose clinical picture is dominated by neuropathic pain. It is unknown if critical illness can affect IENF. METHODS: We enrolled 14 adult neurocritical care patients with prolonged intensive care unit (ICU) stay and artificial ventilation (≥ 3 days), and no previous history or risk factors for neuromuscular disease. All patients underwent neurological examination including evaluation of consciousness, sensory functions, muscle strength, nerve conduction study and needle electromyography, autonomic dysfunction using the finger wrinkling test, and skin biopsy for quantification of IENF and sweat gland innervation density during ICU stay and at follow-up visit. Development of infection, sepsis and multiple organ failure was recorded throughout the ICU stay. RESULTS: Of the 14 patients recruited, 13 (93%) had infections, sepsis or multiple organ failure. All had severe and non-length dependent loss of IENF. Sweat gland innervation was reduced in all except one patient. Of the 7 patients available for follow-up visit, three complained of diffuse sensory loss and burning pain, and another three showed clinical dysautonomia. CONCLUSIONS: Small fiber pathology can develop in the acute phase of critical illness and may explain chronic sensory impairment and pain in neurocritical care survivors. Its impact on long term disability warrants further studies involving also non-neurologic critical care patients.
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spelling pubmed-37871012013-10-04 Small Nerve Fiber Pathology in Critical Illness Latronico, Nicola Filosto, Massimiliano Fagoni, Nazzareno Gheza, Laura Guarneri, Bruno Todeschini, Alice Lombardi, Raffaella Padovani, Alessandro Lauria, Giuseppe PLoS One Research Article BACKGROUND: Degeneration of intraepidermal nerve fibers (IENF) is a hallmark of small fiber neuropathy of different etiology, whose clinical picture is dominated by neuropathic pain. It is unknown if critical illness can affect IENF. METHODS: We enrolled 14 adult neurocritical care patients with prolonged intensive care unit (ICU) stay and artificial ventilation (≥ 3 days), and no previous history or risk factors for neuromuscular disease. All patients underwent neurological examination including evaluation of consciousness, sensory functions, muscle strength, nerve conduction study and needle electromyography, autonomic dysfunction using the finger wrinkling test, and skin biopsy for quantification of IENF and sweat gland innervation density during ICU stay and at follow-up visit. Development of infection, sepsis and multiple organ failure was recorded throughout the ICU stay. RESULTS: Of the 14 patients recruited, 13 (93%) had infections, sepsis or multiple organ failure. All had severe and non-length dependent loss of IENF. Sweat gland innervation was reduced in all except one patient. Of the 7 patients available for follow-up visit, three complained of diffuse sensory loss and burning pain, and another three showed clinical dysautonomia. CONCLUSIONS: Small fiber pathology can develop in the acute phase of critical illness and may explain chronic sensory impairment and pain in neurocritical care survivors. Its impact on long term disability warrants further studies involving also non-neurologic critical care patients. Public Library of Science 2013-09-30 /pmc/articles/PMC3787101/ /pubmed/24098716 http://dx.doi.org/10.1371/journal.pone.0075696 Text en © 2013 Latronico et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Latronico, Nicola
Filosto, Massimiliano
Fagoni, Nazzareno
Gheza, Laura
Guarneri, Bruno
Todeschini, Alice
Lombardi, Raffaella
Padovani, Alessandro
Lauria, Giuseppe
Small Nerve Fiber Pathology in Critical Illness
title Small Nerve Fiber Pathology in Critical Illness
title_full Small Nerve Fiber Pathology in Critical Illness
title_fullStr Small Nerve Fiber Pathology in Critical Illness
title_full_unstemmed Small Nerve Fiber Pathology in Critical Illness
title_short Small Nerve Fiber Pathology in Critical Illness
title_sort small nerve fiber pathology in critical illness
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3787101/
https://www.ncbi.nlm.nih.gov/pubmed/24098716
http://dx.doi.org/10.1371/journal.pone.0075696
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